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A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family.
Genes (Basel). 2021 Nov 6;12(11):1765. doi: 10.3390/genes12111765.
Genes (Basel). 2021.
PMID: 34828371
Free PMC article.
Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes.
Wonkam A, Adadey SM, Schrauwen I, Aboagye ET, Wonkam-Tingang E, Esoh K, Popel K, Manyisa N, Jonas M, deKock C, Nembaware V, Cornejo Sanchez DM, Bharadwaj T, Nasir A, Everard JL, Kadlubowska MK, Nouel-Saied LM, Acharya A, Quaye O, Amedofu GK, Awandare GA, Leal SM.
Wonkam A, et al. Among authors: popel k.
Commun Biol. 2022 Apr 19;5(1):369. doi: 10.1038/s42003-022-03326-8.
Commun Biol. 2022.
PMID: 35440622
Free PMC article.
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Childhood Hearing Impairment in Senegal.
Dia Y, Loum B, Dieng YJKB, Diop JPD, Adadey SM, Aboagye ET, Ba SA, Touré AA, Niang F, Diaga Sarr P, Tidiane Ly CA, Sène ARG, Kock C, Bassier R, Popel K, Ndiaye Diallo R, Wonkam A, Diallo BK.
Dia Y, et al. Among authors: popel k.
Genes (Basel). 2023 Feb 23;14(3):562. doi: 10.3390/genes14030562.
Genes (Basel). 2023.
PMID: 36980833
Free PMC article.
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